Skip to main content

Full text of "USPTO Patents Application 10089810"

See other formats


MAR. 4. 2004 3:56PM 



NO. 1054 P. 7 



Application No. 10/089,810 
Case No. FA 1068 

This listing of claims will replace all prior versions, and listings, of claims in the 
application: 

Listing of Claims: 

Claims 1-9, (canceled) 

Claim 10- (previously presented) A process for coating a clear lacquer coating 
over a base lacquer in a base lacquer/clear lacquer two-coat 
lacquering system, comprising the steps of: 

a) applying a base lacquer coating selected from the group consisting 
of a color-providing base lacquer coating and an effect-providing 
base lacquer coating to a substrate; 

b) applying the clear lacquer coating onto the base lacquer coating as 
a top coating, said clear lacquer coating being curable by radical 
polymerization; and 

c) curing said clear lacquer coating with high-energy radiation; 

wherein the clear lacquer coating comprises a resin solid consisting of: 

I. 70 to 100 of at least one radically polymerizable polymer 
selected from the group consisting of oligomers and prepolymers, 
wherein said polymers have at least one olefinically unsaturated 
group; and 

II. 0 to 30 wt.% of at least one radically polymerizable reactive thinner 
having olefinically unsaturated groups and having a calculated 
molar mass of less than 500; 

wherein 75 to 100 wt.% of component I Is an aliphatic urethane 
(meth)acrylate having an average (meth)acryloyl functional tty of 3 to 
4.5 and a calculated molecular mass of at least 826; 

wherein said aliphatic urethane (meth)acrylate Is fomied by reacting an 
acyclic aliphatic diisocyanate having 8 C atoms with at least one low- 

2 



PAGE 7115 * RCVD AT 3/4/2004 3:47:16 PM [Eastern Standard Time] * SVR:USPT0-EFXRF.1/1 ' DNIS:8729306 * CSID: ' DURATION (mm-ss):07-38 



MAR. 4. 2004 3:56PM 



NO. 1 054 P. 8 



Application No. 10/089,810 
Case No. FA 1068 

molecular aliphatic compound, wherein sard low-molecular aliphatic 
compound has at least one hydroxy group and at least one 
(meth)acryloyl group, and optionally with at least one low-molecular 
aliphatic hydroxy reactant selected from the group consisting of diols 
and polyols; and 

wherein 0 to 25 wt,% of component I is a radically polymerizable 
member selected from the group consrsting of polymers and oligomers, 
wherein said radically polymerizable member contains radically 
polymerizable double bonds, said radically polymerizable member 
being different from the aliphatic urethane (meth)acry late of component 
L 

Claim 1 1 . (previously presented) The process according to claim 1 0 wherein the 
aliphatic urethane (meth)acrylate is formed by reacting polyisocyanates 
based on acyclic aliphatic diisocyanates having 8 C atoms, wherein the 
polyisocyanates contain heteroatom groups linking isocyanate groups 
together in said polyisocyanates, with at least one low-molecular 
aliphatic compound, wherein said low-molecular aliphatic compound 
has at least one hydroxy group and at least one (meth)acry!oyl group, 
and optionally with at least one low-molecular aliphatic hydroxy 
reactant selected from the group consisting of diofs and polyols. 

Claim 12. (previously presented) The process according to claim 10 wherein the 
clear lacquer coating comprises a resin solid consisting of: 

I. 90 to 100 wt.% of at least one radically polymerizable polymer 
selected from the group consisting of oligomers and prepolymers, 
wherein said polymers have at least one olefinically unsaturated 
group; and 

II, 0 to 1 0 wt,% of at least one radically polymerizable reactive thinner 
having olefinically unsaturated groups and having a calculated 
molar mass of less than 500. 



3 



PACE 8/15 ' RCVD AT 3/4/2004 3:47:16 PM [Eastern Standard Time] * SVR:USPT0-EFXRF-1/1 ' DNIS:8729306 * CSID: * DURATION (mm-ss):07-38 



MAR. 4. 2004 3: 57PM NO. 1054 P. 9 

Application No. 1 0/089.81 0 
Case No. FA 1068 

Claim 13. (previously presented) A process for coating a transparent sealing 
coat onto a multi-coat lacquer, comprising the steps of: 

(a) applying the transparent sealing coat to an outer lacquer coating of 
a substrate; and 

(b) curing the transparent sealing coat with high-energy radiation; 

wherein the transparent sealing coat comprises a resin solid consisting 
of: 

I. 70 to 100 wt.% of at least one radically polymeri^able polymer 
selected from the group consisting of oligomers and prepolymers. 
wherein said polymers have at least one olefinically unsaturated 
group; and 

II. 0 to 30 wt.% of at least one radically polymerizable reactive thinner 
having olefinically unsaturated groups and having a calculated 
molar mass of less than 500; 

wherein 75 to 100 wt% of component I is an aliphatic urethane 
(meth)acrylate having an average {meth)acryloyl functionality of 3 to 
4.5 and a calculated molecular mass of at least 826: 

wherein said aliphatic urethane (meth)acrylate is formed by reacting an 
acyclic aliphatic diisocyanate having 8 C atoms with at least one low- 
molecular aliphatic compound, wherein said low-molecular aliphatic 
compound has at least one hydroxy group and at least one 
(meth)acryloyl group, and optionally with at least one low-molecular 
aliphatic hydroxyl reactant selected from the group consisting of diols 
and polyols and 

wherein 0 to 25 wt-% of component I is a radically polymerizable 
member selected from the group consisting of polymers and oligomers, 
wherein said radically polymerizable member contains radically 
polymerizable double bonds, said radically polymerisable member 
being different from the aliphatic urethane (meth)acrylate of component 
I. 

4 



PAGE 9/15 ' RCVD AT 3/4/2004 3:47:16 PM [Eastern Standard Time] ' SVR:USPT0-EFXRF-1/1 ' DNIS:8729306 ' CSID: ' DURATION (mm-ss):07-38 



MAR, 4. 2004. 3: 57PM 



NO. 1054 P. 10 



Application No. 10/089.810 
Case No. FA 1068 



Claim 14. (previously presented) The process according to claim 13 wherein the 
aliphatic urethane (meth)acrylate is formed by reacting polyisocyanates 
based on acyclic aliphatic diisocyanates having 8 C atoms, wherein the 
polyisocyanates contain heteroatom groups linking isocyanate groups 
together in said polyisocyanates, with at least one low-molecular 
aliphatic compound, wherein said low-molecular aliphatic compound 
has at least one hydroxy group and at least one (meth)acryloyl group, 
and optionally with at least one low-molecular aliphatic hydroxyl 
reactant selected from the group consisting of diols and polyols. 

Claim 15. (previously presented) The process according to claim 13 wherein the 
transparent sealing coat comprises a resin solid consisting of: 

I. 90 to 100 wt.% of at least one radically polymerizable polymer 
selected from the group consisting of oligomers and prepolymers, 
wherein said polymers have at least one olefinically unsaturated 
group; and 

II, 0 to 10 wt.% of at least one radically polymerizable reactive thinner 
having olefinically unsaturated groups and having a calculated 
molar mass of less than 500. 

Claim 1 6. (previously presented) The process according to claim 1 0 or 1 3, 

wherein the acyclic aliphatic diisocyanate having 8 C atoms is selected 
from the group consisting of methyl pentane diisocyanate and hexane 
diisocyanate. 

Claim 17. (previously presented) The process according to claim 1 1 or 14. 

wherein the polyisocyanates are selected from the group consisting of 
polyisocyanates with carbodiimide groups, polyisocyanates with 
allophanate groups, polyisocyanates with isocyanurate groups, 
polyisocyanates with uretdione groups, and polyisocyanates with biuret 
groups. 



5 



PAGE 10/1S * RCVD AT 3/4/2004 3:47:16 PM [Eastern Standard Time] * SVR:USPT0-EFXRF-111 * DNIS:8729306 * CSID: * DURATION (mm-ss):07-38 



MAR. 4. 2004 3:58PM 



NO. 1054 P. 11 



Application No. 10/089,810 
Case No- FA 1068 

Claim 18. (previously presented) The process according to claim 11 or 14, 

wherein the polylsocyanates are selected from the groups consisting of 
tris-(6-isocyanatohexyl)-biuret and isocyanurate derived from hexane 
diisocyanate. 

Claim 19. (previously presented) The process according to claim 13 wherein the 
transparent sealing coat is applied in step (a) to an outer lacquer 
coating selected from the group consisting of a single-coat finishing 
lacquer coat, an outer finishing lacquer coat, and an outer clear lacquer 
coat. 

Claim 20. (previously presented) A substrate coated according to the process of 
claim 10, 

Claim 21 . (previously presented) A substrate coated according to the process of 
claim 13. 



Claim 22. (previously presented) The substrate according to claim 20 or 21 
wherein said substrate is a motor vehicle or part thereof. 

Claim 23. (previously presented) The process according to claim 13 wherein said 
transparent sealing coat is applied in step (a) to areas of the outer 
lacquer coating particularly susceptible to scratching. 

Claim 24. (previously presented) The process according to claim 23 wherein said 
transparent sealing coat is applied to areas of a motor vehicle selected 
from the group consisting of areas near locks, areas near door 
handles, areas near door entries, loading edges, roof, and rear end of 
said motor vehicle. 



6 

PAGE 1 1/15 * RCVD AT 31412004 3:47:16 PM [Eastern Standard Time] * SVR:USPT0-EFXRF-1/1 * DNIS:8729306 ' CSID: * DURATION |fnm-ss):07-38